A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456196



Internal ID21113749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84767272..84767829hg38UCSC Ensembl
chr11:84478315..84478872hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994265
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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